| First Author | Hong CS | Year | 2001 |
| Journal | Biochem Biophys Res Commun | Volume | 289 |
| Issue | 4 | Pages | 882-7 |
| PubMed ID | 11735129 | Mgi Jnum | J:73862 |
| Mgi Id | MGI:2156965 | Doi | 10.1006/bbrc.2001.6056 |
| Citation | Hong CS, et al. (2001) Molecular cloning and characterization of mouse cardiac junctate isoforms. Biochem Biophys Res Commun 289(4):882-7 |
| abstractText | Junctate is a newly identified integral ER/SR membrane calcium binding protein, which is an alternative splicing form of the same gene generating aspartyl beta-hydroxylase and junctin. Screening a mouse heart cDNA library using canine junctin cDNA as a probe yielded three complete mouse heart cDNAs. One of the cDNAs is homologous to the previously reported human junctate. The three mouse junctate proteins are composed of 270, 259, and 215 amino acids (we named them junctate-1, -2, and -3). The apparent molecular masses of the mouse junctates in SDS-PAGE were in the range between 40 and 53 kDa. Northern and Western blot analyses indicate that mouse junctates are expressed in heart, brain, spleen, lung, liver, kidney, and stomach, but not in skeletal muscle. The apparent molecular weights of junctates from heart and brain were somewhat different from those from the other tissues tested, suggesting that there are tissue-specific expression patterns of the different junctate isoforms. Immunohistochemical studies showed that junctates were expressed both in ventricular and atrial tissues. This is the first study that shows the presence of 3 distinct cardiac junctate isoforms expressed in various mammalian tissues. |
